Solvent-free enantioselective friedländer condensation with wet 1,1′-Binaphthalene-2,2′-diamine-derived prolinamides as organocatalysts

Journal of Organic Chemistry

Volumn 78, Issue 11, 2013, Pages 5349-5356

  Bañón Caballero, Abraham ^a   Guillena, Gabriela ^a   Nájera, Carmen ^a  

^a UNIVERSITY OF ALICANTE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; AMINES; SILICA; SILICA GEL; SOLVENTS;

CYCLOHEXANONE DERIVATIVES; ELECTRON-DONATING GROUP; ELECTRONWITHDRAWING; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; ENANTIOSELECTIVIES; SEPARABLE MIXTURES; SOLVENT FREE CONDITIONS;

CATALYSTS;

1 ETHYL 2,3 DIHYDRO 1H CYCLOPENTA[B]QUINOLINE; 1 METHYL 2,3 DIHYDRO 1H CYCLOPENTA[B]QUINOLINE; 1,1' NINAPHTHALENE 2,2' DIAMINE DERIVATIVE; 2 (TERT BUTYL) 1,2,3,4 TETRAHYDROACRIDINE; 2 ETHYL 2,3 DIHYDRO 1H CYCLOPENTA[B]QUINOLINE; 2 METHYL 1,2,3,4 TETRAHYDROACRIDINE; 2 PHENYL 1,2,3,4 TETRAHYDROACRIDINE; 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 2 PROPYL 6 (TRIFLUOROMETHYL) 1,2,3,4 TETRAHYDROACRIDINE; 2 [(TERT BUTYLDIMETHYLSILYL)OXY] 1,2,3,4 TETRAHYDROACRIDINE; 5,7 DIBROMO 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 7 (BENZYLOXY) 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 7 CHLORO 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 7 FLUORO 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 7 METHOXY 2 PROPYL 1,2,3,4 TETRAHYDROACRIDINE; 9 PROPYL 8,9,10,11 TETRAHYDROBENZO[C]ACRIDINE; CYCLOHEXANONE DERIVATIVE; ETHYL 1,2,3,4 TETRAHYDROACRIDINE 2 CARBOXYLATE; QUINOLINE DERIVATIVE; TACRINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL REACTION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; FRIEDLANDER REACTION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE;

EID: 84879289024     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400522m     Document Type: Article

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